Jiuzhou

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About Us

新药注册和 MAH 制度下CGMP 生产

- 灵活的多功能生产车间
- 覆盖公斤级到吨级以上的生产线注册起始物料
- 注册中间体及 API 的 CGMP 生产
- 支持批准 NDA 申报的工艺验证
- 拥有 NDA 批准的全球审计经验
- 全球 NDA 注册文件撰写和申报
- 持续工艺改进和商业化生产
- 工艺安全风险评估
- 持续稳定性考察

Other Quality and Compliance

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Jiuzhou
Contact us
Wechat

Business Collaboration

Innovative Drug CDMO Services

Tel: 86-576-85588039

E-mail: bd@jiuzhoupharma.com

Established Business Services（API）

Tel: 86-576-88881561

E-mail: bd@jiuzhoupharma.com

Human Resources

Join Us

Tel: 86-576-88827582

E-mail: hr@jiuzhoupharma.com

Jiuzhou

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